NCT06897423

Brief Summary

This research was planned to examine the effect of disaster midwifery education on the disaster risk perception and self-efficacy levels of midwifery students. The research universe will consist of third-year students studying at the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences University (SBU) in the spring semester of the 2023-2024 academic year (N: 80). In this semi-experimental pre-test and post-test design and control group planned research, in order to determine the sample size; the data were normally distributed, the standard deviation of the main mass was estimated as 1 and the effect size (effect size, difference) as 0.8. For the analysis to be conducted, it was calculated that the highest power value of the research would be 0.942182 in the case of taking two independent n₁=40, n₂=40 samples at a 5% significance level. The G-power analysis result is given below. Students who volunteer to participate in the study will be assigned to the intervention and control groups using the computer-aided simple random sampling method. Computer-aided randomization will be used in the study, and the number of cases will be entered through the program with the URL address https://www.randomizer.org and random assignment will be made to the intervention and control groups. The study will be conducted single-blind. Midwifery students will be administered the "Disaster Risk Perception" and "Self-Efficacy Scale in Disaster Intervention" before and 8 weeks after the first training. Each training period is limited to 60 minutes, once a week.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 7, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

March 5, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 5, 2025

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 15, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

March 26, 2025

Completed
Last Updated

March 26, 2025

Status Verified

December 1, 2024

Enrollment Period

Same day

First QC Date

December 7, 2024

Last Update Submit

March 20, 2025

Conditions

Outcome Measures

Primary Outcomes (3)

  • Introductory Information Form:

    This form, created by researchers based on literature, includes questions about the participants' age, high school graduation, whether they see themselves as sufficient against disasters, etc.

    10 minutes

  • Disaster Risk Perception Scale

    The scale consists of 21 items and 4 dimensions. The scale has four sub-dimensions: "threat", "fatalism", "controllability" and "anxiety". The "threat" sub-dimension of the scale consists of seven items, the "fatalism" sub-dimension consists of three items, the "controllability" sub-dimension consists of six items and the "anxiety" sub-dimension consists of five items. The items in the scale are in a 5-point Likert format as "1- Strongly Disagree", "2- Disagree", "3-Partially Agree", "4-Agree", "5-Strongly Agree". The lowest score that can be obtained from the scale is 21 and the highest is 105. As the score obtained from the scale increases, the level of disaster risk perception increases.

    10 minutes

  • Self-Efficacy Scale in Disaster Response

    The Disaster Response Self-Efficacy Scale, developed by Hong-Yan Li and colleagues in 2017 and Turkish validity security studies conducted by Koca and colleagues in 2018, consists of 19 items and 3 sub-dimensions, and the answers are taken with a 5-point Likert scale. A high score from the scale indicates a high level of disaster response self-efficacy. The scale has three sub-factors. Sub-factors: "On-Site Rescue Competence (Items 1 - 11)", "Disaster Psychological Nurse Competence (Items 12 - 15)" and "The nature of the role undertaken in the disaster and adaptation competence (Items 16 - 19)". The Cronbach alpha coefficient for the entire scale is 0.96. The Cronbach alpha values taken for the sub-dimensions are; on-site rescue competence was determined as 0.93, disaster psychological nurse competence was determined as 0.93, the quality of the role undertaken in the disaster and adaptation competence was determined as 0.93

    10 minutes

Secondary Outcomes (3)

  • Introductory Information Form:

    10 minutes

  • Disaster Risk Perception Scale

    10 minutes

  • Self-Efficacy Scale in Disaster Response

    10 minutes

Study Arms (2)

Intervention group (n:40)

EXPERIMENTAL

Midwifery students in the intervention group of the study will receive 8 weeks of disaster midwifery training. The training content will be covered in 8 main categories: "safe prenatal, delivery and postnatal period", "women's reproductive health services", "family planning", "immunization", "violence and sexually transmitted infections" and "newborn and infant care", "reproductive health in disadvantaged groups", "emergency obstetric situations". The training content will be supported by distributing a 12-page training booklet consisting of these contents to the participants. Each training will be planned for 60 minutes.

Other: Education

Control group (n:40

NO INTERVENTION

no intervention After the research is completed, it is planned to give the same training to the control group.

Interventions

Midwifery students in the intervention group of the study will receive 8 weeks of disaster midwifery training. The training content will be covered in 8 main categories: "safe prenatal, delivery and postnatal period", "women's reproductive health services", "family planning", "immunization", "violence and sexually transmitted infections" and "newborn and infant care", "reproductive health in disadvantaged groups", "emergency obstetric situations".

Intervention group (n:40)

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Volunteer to participate in the research.
  • Health Sciences University, Hamidiye Health Sciences Faculty Midwifery Department Being an active student in the 3rd year.

You may not qualify if:

  • Being a passive student in the 3rd year of the Department of Midwifery, Hamidiye Faculty of Health Sciences, University of Health Sciences.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Educational Status

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assoc. Prof.

Study Record Dates

First Submitted

December 7, 2024

First Posted

March 26, 2025

Study Start

March 5, 2025

Primary Completion

March 5, 2025

Study Completion

March 15, 2025

Last Updated

March 26, 2025

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations